News

CALL FOR PAPERS MAY 2024

IJSAR going to launch new issue Volume 05, Issue 05, May 2024; Open Access; Peer Reviewed Journal; Fast Publication. Please feel free to contact us if you have any questions or comments send email to: editor@scienceijsar.com

IMPACT FACTOR: 6.673

Submission last date: 15th May 2024

Lisch nodules, one of the hallmark manifestations of neurofibromatosis type 1

×

Error message

  • Notice: Trying to access array offset on value of type int in element_children() (line 6609 of /home1/sciensrd/public_html/scienceijsar.com/includes/common.inc).
  • Notice: Trying to access array offset on value of type int in element_children() (line 6609 of /home1/sciensrd/public_html/scienceijsar.com/includes/common.inc).
  • Deprecated function: implode(): Passing glue string after array is deprecated. Swap the parameters in drupal_get_feeds() (line 394 of /home1/sciensrd/public_html/scienceijsar.com/includes/common.inc).
Author: 
Manal Bouggar, Zakaria Chaibi, Houda Brarou, Yassmine Bensaoud, Saif Zineb, Yassine Mouzari and Abdelbare Oubaaz
Page No: 
7270-7271

Von Recklinghausen disease or neurofibromatosis type I (NF1) is the most common phacomatosis. Inherited forms are transmitted in an autosomal dominant fashion. Lisch nodules are the most common ophthalmological manifestation of NF1, reported in 73-95% of cases. We report the case of a 49-year-old female patient, referred to ophthalmology for a systematic ocular check-up in view of the following cutaneous signs: café-au-lait spots and multiple neurofibromas.

Download PDF: